Exploring the role of TGF-β signaling and its crosstalk with other pathways during retina regeneration in Danio rerio
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IISERM
Abstract
Any injury to retina leads to irreparable damage in mammals. Unlike higher vertebrates,
zebrafish possess remarkable regenerative response in retina, driven by Müller Glia (MG),
the only glial cell type in retina. Upon retinal injury, the Müller Glia cells undergo de-
differentiation and cell division to give rise to a population of MGPCs (Müller Glia
derived Progenitor cells), which migrate to damaged layers of retina to differentiate and
restore cell population. But the exact mechanism of molecular interplay that orchestrates
de-differentiation, proliferation and re-differentiation still remains elusive. Although many
signaling cascades and regulatory pathways have been identified to play roles at different
stages of retina regeneration, TGF-β signaling pathway remains under-explored. In this
study, we analysed the role of a developmentally important signaling pathway i.e. TGF-β
signaling in the retina regeneration. Also, we explored the communication that TGF-β
pathway has with other signaling pathways. We found that TGF-β signaling and Notch
signaling interplay is important for retina regeneration. Another signaling that we
explored is Shh(Sonic Hedgehog), which is one of the major networks that regulates the
key events during developmental processes. We tried to understand how TGF-β signaling
is communicating with Notch and Shh signaling to help restore the structural and
functional integrity of the retina.